LEVELERT II FLUID LEVEL SENSOR— 510(k) K060123
Substantially EquivalentSmith & Nephew, Inc.
FDA 510(k) clearance K060123 for LEVELERT II FLUID LEVEL SENSOR, Substantially Equivalent on 2006-02-14. Applicant: Smith & Nephew, Inc.. Device class: 2.
Clearance details
- Applicant
- Smith & Nephew, Inc.
- Product code
- Code FLN
- Device class
- Class 2
- Regulation
- 21 CFR 880.2420
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Andover, MA, US
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